US4025552A - 3-(4'-Alkoxy-benzoyl)-1,2,2-trimethylcyclopentane-carboxylic acids, methods of use and compositions containing such compounds - Google Patents
3-(4'-Alkoxy-benzoyl)-1,2,2-trimethylcyclopentane-carboxylic acids, methods of use and compositions containing such compounds Download PDFInfo
- Publication number
- US4025552A US4025552A US05/540,504 US54050475A US4025552A US 4025552 A US4025552 A US 4025552A US 54050475 A US54050475 A US 54050475A US 4025552 A US4025552 A US 4025552A
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- US
- United States
- Prior art keywords
- compounds
- benzoyl
- alkoxy
- compound
- trimethylcyclopentane
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 150000001875 compounds Chemical class 0.000 title claims description 26
- 239000000203 mixture Substances 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 5
- 230000002891 anorexigenic effect Effects 0.000 claims description 7
- 241001465754 Metazoa Species 0.000 claims description 5
- SRACYVZIGUOQNK-UHFFFAOYSA-N 3-(3,4-dimethoxybenzoyl)-1,2,2-trimethylcyclopentane-1-carboxylic acid Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)C1C(C)(C)C(C)(C(O)=O)CC1 SRACYVZIGUOQNK-UHFFFAOYSA-N 0.000 claims description 2
- OKBKFSVXFIEVNE-UHFFFAOYSA-N 3-(4-ethoxybenzoyl)-1,2,2-trimethylcyclopentane-1-carboxylic acid Chemical compound C1=CC(OCC)=CC=C1C(=O)C1C(C)(C)C(C)(C(O)=O)CC1 OKBKFSVXFIEVNE-UHFFFAOYSA-N 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 230000001939 inductive effect Effects 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 abstract description 4
- 239000002830 appetite depressant Substances 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 9
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 4
- JZMUCLZEZUFWDA-UHFFFAOYSA-N 3-(4-methoxybenzoyl)-1,2,2-trimethylcyclopentane-1-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C(=O)C1C(C)(C)C(C)(C(O)=O)CC1 JZMUCLZEZUFWDA-UHFFFAOYSA-N 0.000 description 3
- VFZDNKRDYPTSTP-UHFFFAOYSA-N 5,8,8-trimethyl-3-oxabicyclo[3.2.1]octane-2,4-dione Chemical compound O=C1OC(=O)C2(C)CCC1C2(C)C VFZDNKRDYPTSTP-UHFFFAOYSA-N 0.000 description 3
- 241000282472 Canis lupus familiaris Species 0.000 description 3
- 150000005224 alkoxybenzenes Chemical class 0.000 description 3
- 229940125904 compound 1 Drugs 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 230000037396 body weight Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000699670 Mus sp. Species 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/76—Unsaturated compounds containing keto groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C62/00—Compounds having carboxyl groups bound to carbon atoms of rings other than six—membered aromatic rings and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C62/30—Unsaturated compounds
- C07C62/38—Unsaturated compounds containing keto groups
Definitions
- the invention relates to new compounds, their optical isomers, to a process of preparation thereof and to drugs containing such compounds.
- the compounds according to the invention are formed by the 3-(4'-alkoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acids of formula ##STR1## in which OR represents 1 or 2 alkoxy groups fixed on the phenyl group, said alkoxy group being either methoxy or ethoxy groups.
- the invention also relates to the optical isomers of these compounds, more particularly to the isomers thereof.
- the process according to the invention makes use of a condensation of the FRIEDEL & CRAFTS type, in the presence of aluminum chloride as a catalyst.
- camphoric anhydrid of formula: ##STR2## camphoric anhydrid of formula: ##STR2## with the corresponding alkoxy-benzene in the presence of aluminum chloride.
- the alkoxy-benzene and the camphoric anhydride are added in the form of a mixture to the aluminum chloride, or conversely. If need be said mixture is used in the form of a solution in a common organic solvent such as nitrobenzene or tetrachlorethane.
- the isomers of the compounds according to the invention are obtained, in the above process, when starting from the corresponding optical isomers of the camphoric anhydrid.
- reaction is carried out substantially as in example 1, starting however from the dextrorotatory isomer of camphoric anhydride. 10 gr. of the compound are obtained in the form of white crystals which, after crystallisation in benzene, have a melting point of 165°-166° C.
- racemic compound is obtained starting from the racemic form of camphoric anhydride. Its melting point is of 165°-166° C.
- the compounds according to the invention and their isomers exhibit marked therapeutical properties, particularly anorexigenic properties, as has been shown by pharmacological tests on dogs and rats.
- the compound and isomers according to the invention are substantially devoid of toxicity.
- Tests were performed on dogs (female Beagle dogs) having an average weight of 10 kg. and which received 100 mg/kg. of compound 1. 30 minutes thereafter they were presented their usual food, but ate less than the third of the average amount of food eaten by controls. The above dose of compound 1 was perfectly tolerated by the animals. It did not induce any substantial change in their general behaviour.
- a reduction of the amount of food eaten was observed from the first day.
- a reduction of the body weight started on the third day.
- mice, for compound 1 were as follows:
- the compounds and the isomers according to the invention are useful for the treatment of obesity and of excess weight. They are useful for inducing a reduction of the amount of food absorbed by man or animal. They are anorexigen compounds. They can be used as such, or in the form of their physiologically acceptable salts. They are preferably absorbed orally, in admixture either with a solid pharmaceutical carrier or with an orally acceptable solvent.
- the invention also relates to the solid pharmaceutical compositions containing said compounds and to the drinkable solutions of said compounds.
- Daily doses of about 0.200 to about 1 gr., for instance 0.250 gr. can be used. They may be used under dosage units of 0.100 to 0.500 gr.
- the invention is also particularly concerned with the compositions containing the compounds according to the invention, in association with suppository carriers, as well as with the injectable solutions containing said compounds in association with an injectable sterile liquid.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Emergency Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
The invention relates to 3-(4'-alkoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acids, and to their optical isomers; they are useful as active principles for anorexigenic drugs.
Description
The invention relates to new compounds, their optical isomers, to a process of preparation thereof and to drugs containing such compounds.
The compounds according to the invention are formed by the 3-(4'-alkoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acids of formula ##STR1## in which OR represents 1 or 2 alkoxy groups fixed on the phenyl group, said alkoxy group being either methoxy or ethoxy groups.
The invention also relates to the optical isomers of these compounds, more particularly to the isomers thereof.
These compounds exhibit important anorexigenic properties, which are all the more unexpected as they contain only carbon, hydrogen and oxygen, whereas, usually, the known anorexigenic compounds also contain nitrogen in their molecule.
The process according to the invention makes use of a condensation of the FRIEDEL & CRAFTS type, in the presence of aluminum chloride as a catalyst.
More particularly, it consists in reacting camphoric anhydrid of formula: ##STR2## with the corresponding alkoxy-benzene in the presence of aluminum chloride.
Advantageously, the alkoxy-benzene and the camphoric anhydride are added in the form of a mixture to the aluminum chloride, or conversely. If need be said mixture is used in the form of a solution in a common organic solvent such as nitrobenzene or tetrachlorethane.
The isomers of the compounds according to the invention are obtained, in the above process, when starting from the corresponding optical isomers of the camphoric anhydrid.
The invention is hereafter illustrated by examples which have no limitative character.
The preparation of the levorotatory 3-(4'-methoxy benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acid (compound 1):
10 GR. (0.055 MOLE) OF 1-CAMPHORIC ANHYDRID
(α.sub.D.sup.20.sup.° C. = 3.2°)
are dissolved under stirring in 162 gr. (1.5 mole) of methoxy-benzene.
14.6 GR. (0.11 MOLE) OF ALUMINUM CHLORIDE ARE ADDED PORTIONWISE, AT AMBIENT TEMPERATURE AND UNDER STIRRING, TO THE ABOVE SOLUTION. After 2 hours of stirring, the reaction mixture is decomposed by ice and a 10% solution of sulphuric acid. The mixture is extracted with ether (in toto 350 ml) and the total ether solution recovered is washed with water. The ether solution is thereafter treated with 100 ml of a 2% aqueous solution of sodium hydroxyde. The alkaline solution obtained is acidified at pH3 with an acid solution, in the present case hydrochloric acid. The crude compound which is isolated is crystallized in benzene. 10 gr. of the above identified isomer are obtained in the form of white crystals. The physical constants of the product according to the invention are as follows:
M p = 176°
[α]d 20.sup.° c. = 20°, 2 (1= 1; c = 3, chloroform)
main bands in infra-red in cm- 1 (KBr pellet): 2960, 1690, 1650, 1590, 1235, 1170, 840, 600.
Preparation of the dextrorotatory 3-(4'-methoxy benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acid (compound 2).
The reaction is carried out substantially as in example 1, starting however from the dextrorotatory isomer of camphoric anhydride. 10 gr. of the compound are obtained in the form of white crystals which, after crystallisation in benzene, have a melting point of 165°-166° C.
Preparation of the racemic compound of 3-(4'-methoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acid (compound 3).
In the same manner, the racemic compound is obtained starting from the racemic form of camphoric anhydride. Its melting point is of 165°-166° C.
One prepares in the same manner, starting each time from the corresponding alkoxybenzene, the following compounds: 3-(4'-ethoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acid: MP = 122° C. (compound 4)
3 3-(3', 4'-dimethoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acid: MP = 154° C. (compound 5).
The compounds according to the invention and their isomers exhibit marked therapeutical properties, particularly anorexigenic properties, as has been shown by pharmacological tests on dogs and rats.
The compound and isomers according to the invention are substantially devoid of toxicity.
Tests were performed on dogs (female Beagle dogs) having an average weight of 10 kg. and which received 100 mg/kg. of compound 1. 30 minutes thereafter they were presented their usual food, but ate less than the third of the average amount of food eaten by controls. The above dose of compound 1 was perfectly tolerated by the animals. It did not induce any substantial change in their general behaviour.
Similar tests were run on male rats of the Wistar type, having an average weight of 150 g. They were divided in groups (each of which comprised 10 animals) which were given orally the compounds 1, 2, 3, 4, and 5 respectively, in the form of a 1% solution of the tested conpounds, at a dose of 1 ml/ 100 gr. of body weight, during 5 days.
A reduction of the amount of food eaten was observed from the first day. A reduction of the body weight started on the third day.
The L D 50 obtained on mice, for compound 1, were as follows:
orally: 5 gr/kg
intraperitoneally: 500 mg/kg
intraveneously: 125 mg/kg
The compounds and the isomers according to the invention are useful for the treatment of obesity and of excess weight. They are useful for inducing a reduction of the amount of food absorbed by man or animal. They are anorexigen compounds. They can be used as such, or in the form of their physiologically acceptable salts. They are preferably absorbed orally, in admixture either with a solid pharmaceutical carrier or with an orally acceptable solvent.
Therefore, the invention also relates to the solid pharmaceutical compositions containing said compounds and to the drinkable solutions of said compounds.
Daily doses of about 0.200 to about 1 gr., for instance 0.250 gr. can be used. They may be used under dosage units of 0.100 to 0.500 gr.
They can also be administered by the rectal route or by the parenteral route. The invention is also particularly concerned with the compositions containing the compounds according to the invention, in association with suppository carriers, as well as with the injectable solutions containing said compounds in association with an injectable sterile liquid.
Claims (5)
1. A compound having the formula; ##STR3## wherein OR represents a member of the group consisting of 3', 4'-dimethoxy, 3', 4'-diethoxy and 4'-ethoxy.
2. 3-(4'-ethoxy-benzoyl)-1,2,2-trimethylcyclopentane-carboxylic acid.
3. 3-(3',4'-dimethoxybenzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acid.
4. A method for inducing an anorexigenic condition in man or animal which comprises administering to said man or animal an anorexigenic amount of a compound according to claim 1.
5. An anorexigenic composition comprising an anorexigenic amount of a compound having the formula: ##STR4## wherein OR represents a member of the group consisting of 3', 4'-dimethoxy, 3', 4'-diethoxy, 4'-methoxy and 4'-ethoxy in association with a pharmaceutically acceptable carrier.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/705,535 US4113960A (en) | 1975-01-13 | 1976-07-15 | 3-(4'-Alkoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acids, their optical isomers and drugs containing such compounds |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR74.01614 | 1974-01-17 | ||
| FR7401614A FR2270856B1 (en) | 1974-01-17 | 1974-01-17 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/705,535 Continuation-In-Part US4113960A (en) | 1975-01-13 | 1976-07-15 | 3-(4'-Alkoxy-benzoyl)-1,2,2-trimethyl-cyclopentane-carboxylic acids, their optical isomers and drugs containing such compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4025552A true US4025552A (en) | 1977-05-24 |
Family
ID=9133622
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US05/540,504 Expired - Lifetime US4025552A (en) | 1974-01-17 | 1975-01-13 | 3-(4'-Alkoxy-benzoyl)-1,2,2-trimethylcyclopentane-carboxylic acids, methods of use and compositions containing such compounds |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4025552A (en) |
| BE (1) | BE824505A (en) |
| CH (1) | CH591414A5 (en) |
| DE (1) | DE2501834C2 (en) |
| ES (1) | ES433860A1 (en) |
| FR (1) | FR2270856B1 (en) |
| GB (1) | GB1501201A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7655699B1 (en) | 1992-04-22 | 2010-02-02 | Eisai Inc. | Compounds having selective activity for retinoid X receptors, and means for modulation of processes mediated by retinoid X receptors |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2481270A1 (en) * | 1980-04-24 | 1981-10-30 | Roussel Uclaf | NOVEL SUBSTITUTED DERIVATIVES OF 4-PHENYL 4-OXO 2-HYDROXY BUTANOIC ACID, PROCESS FOR THEIR PREPARATION AND APPLICATIONS AS MEDICAMENTS |
| FR2481118A1 (en) * | 1980-04-24 | 1981-10-30 | Roussel Uclaf | APPLICATION AS MEDICAMENTS OF DERIVATIVES SUBSTITUTED WITH PHENYL-4-OXO-2-BUTENOIC ACID |
| FR2504005A2 (en) * | 1980-04-24 | 1982-10-22 | Roussel Uclaf | 4-Substd. phenyl 4-oxo-2-butenoic acids - useful for treatment of digestive tract disorders |
| FR2504004A1 (en) | 1981-04-17 | 1982-10-22 | Roussel Uclaf | APPLICATION AS MEDICAMENTS OF PHENYL ALIPHATIC CARBOXYLIC ACID DERIVATIVES |
| IT1210582B (en) * | 1981-10-22 | 1989-09-14 | Roussel Maestretti Spa | 4-FENYL-4-OSSOBUTEN-2-OICO ACID DERIVATIVES EQUIPPED WITH PHARMACOLOGICAL PROPERTIES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
| FR2515037A1 (en) * | 1981-10-22 | 1983-04-29 | Roussel Uclaf | AS MEDICINES, CERTAIN MONO-SUBSTITUTED DERIVATIVES OF 4-PHENYL 4-OXO BUTEN-2-OIC ACID, AND THE COMPOSITIONS CONTAINING SAME |
| IT1171605B (en) * | 1981-10-22 | 1987-06-10 | Roussel Maestretti Spa | PHARMACOLOGICALLY ACTIVE 4-FENYL-4-OSSOBUTEN-2-OIC ACID DERIVATIVES AND PROCEDURE FOR THEIR PREPARATION |
| SE454355B (en) * | 1983-01-24 | 1988-04-25 | Roussel Uclaf | ACRYLIC ACID DERIVATIVES CONTAINING A FURYL, PYRANYL, BENZOFURANYL, OXAZOLYL OR ISOXAZOLYL GROUP, PROCEDURES FOR PREPARING THEREOF, AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEMSELVES |
| IT1169783B (en) * | 1983-08-25 | 1987-06-03 | Roussel Maestretti Spa | DERIVATIVES OF 4-FENYL 4-BONE-BUTEN 2-OICO ACID, THEIR PREPARATION PROCEDURE AND THEIR APPLICATION AS MEDICINAL PRODUCTS |
| EP0253501A3 (en) * | 1986-07-16 | 1990-04-04 | Imperial Chemical Industries Plc | N-disubstituted cycloalkylmethyl amines useful as fungicides |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2132675A (en) * | 1937-04-08 | 1938-10-11 | Rohm & Haas | Acylated ethers and process for making same |
| US3217033A (en) * | 1962-04-17 | 1965-11-09 | Merck & Co Inc | Process for preparing ortho substituted benzoic acid compounds |
| US3624210A (en) * | 1966-07-27 | 1971-11-30 | Ortho Pharma Corp | Antifertility agent |
| US3702853A (en) * | 1970-01-13 | 1972-11-14 | Syntex Corp | Certain 5-substituted tetrahydroiso-benzofuran-1-ones |
| US3862239A (en) * | 1967-08-22 | 1975-01-21 | Ortho Pharma Corp | Aryl substituted cyclohexenecarbinols |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2618653A (en) * | 1952-11-18 | Cyclohexyl methyl ketones | ||
| DE970480C (en) * | 1940-05-15 | 1958-09-25 | Knoll Ag | Process for the preparation of ª-cyclohexylisopropylmethylamine |
| US3182061A (en) * | 1961-03-20 | 1965-05-04 | Warner Lambert Pharmaceutical | 5-[4-(p-hydroxyphenoxy)phenyl]-5-oxo-3-methylvaleric acid |
-
1974
- 1974-01-17 FR FR7401614A patent/FR2270856B1/fr not_active Expired
-
1975
- 1975-01-13 US US05/540,504 patent/US4025552A/en not_active Expired - Lifetime
- 1975-01-14 CH CH39375A patent/CH591414A5/xx not_active IP Right Cessation
- 1975-01-16 ES ES433860A patent/ES433860A1/en not_active Expired
- 1975-01-17 GB GB2198/75A patent/GB1501201A/en not_active Expired
- 1975-01-17 DE DE2501834A patent/DE2501834C2/en not_active Expired
- 1975-01-17 BE BE152477A patent/BE824505A/en not_active IP Right Cessation
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2132675A (en) * | 1937-04-08 | 1938-10-11 | Rohm & Haas | Acylated ethers and process for making same |
| US3217033A (en) * | 1962-04-17 | 1965-11-09 | Merck & Co Inc | Process for preparing ortho substituted benzoic acid compounds |
| US3624210A (en) * | 1966-07-27 | 1971-11-30 | Ortho Pharma Corp | Antifertility agent |
| US3862239A (en) * | 1967-08-22 | 1975-01-21 | Ortho Pharma Corp | Aryl substituted cyclohexenecarbinols |
| US3702853A (en) * | 1970-01-13 | 1972-11-14 | Syntex Corp | Certain 5-substituted tetrahydroiso-benzofuran-1-ones |
Non-Patent Citations (1)
| Title |
|---|
| Bleazard et al., "J. Org. Chem.", 1961, pp. 68-73. * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7655699B1 (en) | 1992-04-22 | 2010-02-02 | Eisai Inc. | Compounds having selective activity for retinoid X receptors, and means for modulation of processes mediated by retinoid X receptors |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2270856B1 (en) | 1978-07-21 |
| DE2501834A1 (en) | 1975-07-24 |
| BE824505A (en) | 1975-07-17 |
| CH591414A5 (en) | 1977-09-15 |
| DE2501834C2 (en) | 1987-01-08 |
| FR2270856A1 (en) | 1975-12-12 |
| GB1501201A (en) | 1978-02-15 |
| ES433860A1 (en) | 1976-11-16 |
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